Health economic evaluations of non-pharmacological interventions for persons with dementia and their informal caregivers: a systematic review

A systematic literature review was performed, searching the following key databases: Centre for Reviews and Dissemination (National Health Service Economic Evaluation Database; Health Technology Assessment), Cochrane Library, EconLit (EBSCO), Embase (OvidSP), PsycINFO (EBSCO) and PubMed (Medline). The timeframe for electronic searches was restricted to publications from 2010 to 2016. Key words concerning the dementia syndrome such as “dementia”, “Alzheimer’s Disease” etc. were combined with search terms in the context of economic evidence as, for instance, “cost”, “economic evidence”, “cost-utility” “cost-effectiveness” and “savings”. The complete research strategies for the respective databases are presented in the Additional file 1. Unpublished or grey literature was not included. The search was limited to studies in English or German.

Study eligibility was based on title and abstract screening, performed by two independent reviewers. A third independent reviewer was consulted in any case of disagreement. Articles passing the initial screening were retrieved for a detailed full text evaluation. The selection criteria are presented in Table 1.

This review includes studies based on standard economic evaluation methods. Cost-effectiveness analysis (CEA) measures and compares consequences in terms of an appropriate single natural effect or effect on a physical unit, which is common to all considered alternatives. The ratio of the mean incremental cost and the mean incremental effect of the interventions under evaluation is called incremental cost-effectiveness ratio (ICER). The ICER represents a summary measure that may support the decision making process by indicating the cost per unit change with respect to the evaluated outcome [15].

By contrast, cost-utility analysis (CUA) enables a comparison of multiple effects that are not necessarily common to the evaluated alternatives, as multi-dimensional health outcomes are captured into a single index [16]. In CUA health state preference scores (utility values) are used to value the states of health associated with the respective consequences of the interventions. Quality-adjusted life-years (QALY), which combine morbidity and mortality are the most frequently employed outcome measure in CUA [15].

Data extraction was performed in line with the recommendation of the Centre for Reviews and Dissemination for reviews of economic evaluations [17], including type of economic evaluation, study objective, description of the intervention and comparators, measure of benefit, cost data and respective sources, methods for dealing with uncertainty as well as cost and outcome results.

The appraisal of study quality was based on Drummond’s ten-item check-list for assessing economic evaluations [see Additional file 2] [15].

The systematic literature search identified 10,047 publications [see Additional file 1]. After the removal of duplicates, title screening of 6,835 articles was conducted. Subsequent to the screening of 390 abstracts, 37 articles were retrieved in order to assess the full texts. Of these, 16 were included in the synthesis. The flow of articles retrieved through electronic searches is depicted in Fig. 1.

The largest part of the included studies was conducted in the United Kingdom (seven studies). Of these, two articles are based on results from the British START (STrAtegies for RelaTives) study [18, 19]. Three studies were from the United States of America and two were from Finland. Further, one study each was conducted in Canada, the Netherlands, Denmark and Sweden.

Two articles report data on interventions that are mainly targeted at PwDs [20, 21], whereas seven studies comprise interventions, which involve both the PwD and the respective caregiver [22‐28]. Six publications deal with programs that assist caregivers of PwDs [18, 19, 29‐32]. Solely one study was targeted at PwMCI [33].

The identified studies were grouped based on a classification proposed in the World Alzheimer Report 2011 [34].

Non-pharmacological interventions addressed to PwDs and, if applicable, to the patient-caregiver dyads were classified into the following categories:

Moreover, interventions that primarily target caregivers were classed together.

Two trial-based CEA evaluating physical exercise interventions for PwDs [20, 28] and one for PwMCI were identified [33]. The exercise programs of the reviewed CEAs pursue different therapeutic goals, namely the reduction of behavioral and psychological symptoms of dementia (BPSD) [28] or the delay in the deterioration of patient’s physical functioning [20]. The intervention evaluated by Davis et al. [33] aims to improve executive cognitive functions in PwMCI. These different therapeutic goals are also reflected in the range of employed effectiveness measures (see Table 2).

In Finland a CEA was conducted concurrently with the Finnish Alzheimer disease exercise trial (FINALEX) [20]. In the first study arm a one-year group exercise program for community-dwelling persons with AD provided twice a week during visits to day care centers was assessed. The second arm included a one-year tailored home-based exercise program administered twice a week by physiotherapists. Both interventions were compared to a control group obtaining care as usual (CAU). To measure the impact of these intense and long term exercise programs on the physical functioning and mobility of the persons with AD, the Functional Independence Measure (FIM) and the Short Physical Performance Battery (SPPB) were used. Health outcomes were measured at baseline and after three, six and 12 months. Cost data was retrieved for the patient-caregiver dyads from central registries and medical records over a period of 24 months. Pitkälä and colleagues [20] came to the conclusion that an intensive and long-term exercise program administered in the patient’s home could slow the decline in physical functioning without increasing total health and social service costs.

A CEA conducted by D’Amico et al. [28] evaluated an intervention targeting community-dwelling PwDs who showed at least one BPSD. The intervention under evaluation was composed of a 12-week daily walking program (lasting for 20 to 30 min) performed by the patient-caregiver dyad in the surrounding of their residence. The dyads were instructed by a qualified exercise professional. The program was designed to become increasingly more intense, whereas the control group received CAU. The reduction in BPSDs was measured by means of the Neuropsychiatric Inventory (NPI) as the primary effectiveness outcome. Secondary analyses considered the impact on quality of life of the participants with dementia (measured using the DEMQOL-Proxy), caregiver burden (collected by employing the Zarit Caregiver Burden Interview (ZBI)) and caregivers’ mental health (measured using the General Health Questionnaire (GHQ)). Further, QALYs were estimated based on DEMQOL-Proxy scores. A subsample of 52 dyads was analyzed within the framework of the economic analyses [28]. In contrast to the entire sample [35], the economic subsample indicated a statistically significant between-group difference considering the average scores of the GHQ at 12 weeks, favoring the intervention group. The other evaluated outcomes did not show a significant difference at follow-up. The Client Service Receipt Inventory (CSRI) was completed by the caregiver in order to gather data on resource utilization. From the viewpoint of the health and social care system, the intervention group showed lower costs compared to the CAU control group, hence the intervention was dominant; however these results were not statistically significant. From a societal viewpoint, the ICER was estimated to amount to £421 per unit change in the NPI score. Assuming that a reduction of at least three points in the NPI score would be considered clinically relevant, the authors derived the suggestion that a clinically meaningful improvement could be achieved at a cost of £1,263. Therefore D’Amico et al. [28] concluded that the individually tailored walking program is potentially cost-effective when considering BPSD; however they also point to the fact that for the NPI no cost-effectiveness threshold was yet defined. The ICER for QALY was high, thus the intervention seems not to be cost-effective with regard to QALY gains.

In a Canadian three-arm trial, Davis et al. [33] assessed the cost-effectiveness of resistance training and aerobic training compared to a control group receiving balance and tone classes targeted at community dwelling women aged 70 to 80, who self-reportedly expressed to experience memory problems. As primary effectiveness outcome measure the executive cognitive function of selective attention and conflict resolution was assessed by means of the Stroop Test. From the point of view of the Canadian healthcare system, the incremental cost per incremental Stroop change score showed that aerobic training as well as resistance training decreased healthcare costs and proved to be more effective than twice weekly balance and tone classes. The study was limited by the fact that the participants did not have a formal mild cognitive impairment diagnosis. Moreover, the resource use data was collected through a self-completed questionnaire, which might have caused a recall bias.

Three British RCTs were included that evaluated strategies to support and enhance cognition in PwDs [21, 26, 27]. The main considered outcomes were cognition and health-related quality of life (see Table 3).

Orgeta et al. [27] assessed structured, individual, home-based cognitive stimulation sessions for PwDs, administered by the respective caregiver. The caregivers were trained at home by researchers who also provided support via additional home visits or via telephone. Carers received a range of materials such as a manual, an activity workbook and a toolkit comprising boules and playing cards. The program was composed of 75 themed activity sessions. The sessions were designed to last 30 min and were scheduled to be delivered three times a week, over a period of 25 weeks. Compared to treatment as usual, the individual cognitive stimulation therapy (iCST) did not significantly improve cognition (measured by the Alzheimer’s Disease Assessment Scale-Cognition subscale (ADAS-Cog)) or quality of life of the PwD (assessed by the Quality of Life in Alzheimer’s Disease scale (QoL-AD)). This also applies for the caregivers’ physical and mental health (assessed by the Short Form questionnaire-12 items (SF-12)). Intervention costs were offset by some reductions in social care and other services. Even though improvements were neither observed with regard to most of the secondary outcomes for PwDs (activities of daily living, depression and BPSD), analyses indicated that PwDs in the intervention group may experience a higher relationship quality with their caregiver. From the health and social care perspective as well as from the societal perspective, there was no significant between-group difference with regard to mean costs. The authors concluded that considering the primary outcomes, from either perspective, the structured home-based cognitive stimulation does not seem to be more cost-effective than CAU. Further, the researchers remark that there are no available societal willingness-to-pay thresholds for the improvement in the primary outcomes measured by ADAS-Cog, QoL-AD or the Quality of Caregiver-Patient Relationship (QCPR) instrument. Considering the QALY gain for caregivers derived from the EQ-5D with societal weights, iCST was found to be more effective than CAU.

In another trial D’Amico et al. [21] evaluated the cost-effectiveness of a weekly maintenance cognitive stimulation therapy (MCST) over a period of 24 weeks compared to treatment as usual. Before entering the study, all participants completed seven weeks of twice-weekly standard cognitive stimulation therapy [36]. At six months, no difference between the control and intervention group was found with regard to the primary outcome cognition (measured by ADAS-Cog). However, the second primary outcome self-rated quality of life (assessed by means of the QoL-AD) was found to be higher in the intervention group compared to the CAU group. Participants receiving CAU showed only slightly non-significantly lower health and social care costs than participants in the MCST intervention group. The estimated ICER demonstrates that the mean cost for a 1 point difference on the QoL-AD scale was £266. The respective cost-effectiveness acceptability curve (CEAC) indicates that MCST can be considered cost-effective with a probability of 90% at a willingness-to-pay of around £1,400. In contrast, this probability was low considering cognition as outcome. Even though no significant between-group difference on the Mini-Mental Status Examination (MMSE) score was observed, the CEA indicated that MCST is likely to be cost-effective considering MMSE as outcome measure. Considering QALY gains derived from EQ-5D proxy-ratings, the mean incremental cost-utility ratio (ICUR) was £26,835. At a threshold of £20,000, CEAC suggests that considering the former outcome the probability of cost-effectiveness was 40%. Sensitivity analyses conducted from the societal perspective yielded inconsistent cost-effectiveness findings.

Within the framework of the REMCARE trial Woods et al. [26] evaluated the cost-effectiveness of weekly joint reminiscence groups provided for PwDs and their caregivers over a time span of 3 months, followed by monthly maintenance sessions over a period of 7 months. Primary outcomes were the PwD’s quality of life (measured by the QoL-AD) and carer’s mental health (assessed by the General Health Questionnaire-28 (GHQ-28)). With regard to these primary outcomes neither after 3 months nor after 10 months significant group-difference could be found. After 10 months, caregivers assigned to the intervention group even showed a significant increase in anxiety. Considering the mean health and social service costs for PwDs, the mean total costs for the intervention group was found to be 13.5% higher compared to the control group. However this between-group difference was not statistically significant. The estimated ICER for the QoL-AD was £2,586 (CI: -20,280 to 24,340). Woods et al. [26] concluded that the intervention was neither effective nor cost-effective.

Three publications evaluated psychological and behavioral therapies delivered to PwD-caregiver dyads (see Table 4) [22, 24, 25].

A pilot RCT conducted by Spector et al. [25] in the UK assessed the cost of a ten-session cognitive-behavioral therapy (CBT) for patient-caregiver dyads compared to treatment as usual from the health and social care perspective. The Rating Anxiety in Dementia scale (RAID) was used as the primary outcome measure. The cost analysis yielded that at 15 weeks the adjusted difference in anxiety of the PwDs was lower in the CBT group compared to the control group ( -3.10; 95% CI: -6.55 to 0.34). This finding was maintained at 6 months ( -4.59; 95% CI: -9.34 to 0.15). Further, at 15 weeks depression of the PwDs measured by the adjusted Cornell Scale for Depression in Dementia (CSDD) was lower in the CBT group ( -5.37; 95% CI: -9.50 to -1.25), which remained significant at 6 months. The total cost that occurred over the 6-month follow-up period were found to be significantly lower within the CBT group compared to CAU (adjusted mean difference -£564.38 (95% CI: -£1,252.08 to -£112.85)). While also including intervention cost, estimated to amount to £1,002 per person, the total cost from the health and social service perspective were lower for the control group, with an adjusted mean difference of £769.80 (95% CI: -£121.99 to £1,697.38). However, this difference was not found to be statistically significant. Hence, the authors concluded that CBT proved to be cost neutral.

A Finnish trial conducted by Laakkonen et al. [24] performed a CEA, evaluating a self-management group rehabilitation program for PwDs and their spouses administered shortly after the diagnosis. The intervention comprised eight group sessions of self-management offered to the spousal dyads and was compared to CAU. At 3-month, the intervention group demonstrated higher HRQoL outcomes as measured with the Finnish version of the RAND 36-Item Health Survey in spouses of PwD, however after 9 months the effect was weakened. With respect to spouses’ sense of competence and feelings of mastery (assessed by the Sense of Competence Questionnaire (SCQ)) no significant group difference was demonstrated. Further, cognitive scores of PwDs in the intervention group improved significantly more than those of the control group. These positive effects were not accompanied with higher health and social services costs; hence the authors concluded that the self-management group rehabilitation is cost neutral.

As part of the Danish Alzheimer’s Intervention Study, which assessed the provision of an early psychosocial intervention for community-dwelling PwDs with a recent diagnosis and their respective caregivers, a CUA was conducted from the societal perspective. Søgaard and his colleagues [22] evaluated an intensive, multicomponent, semi-tailored psychosocial intervention program over a period of 3 years. The program was composed of counselling, educational and support elements, which were compared to a control group that was informed about available support programs in their respective communities [37]. QALY were estimated individually for the PwD and the respective caregiver and eventually aggregated for the analysis. HRQoL values of the PwDs were measured by means of proxy-rated EQ-5D. Cost data on informal care and production loss was collected by means of the Resource Utilization in Dementia (RUD) instrument. Data on resource utilization in the primary and secondary health sector was based on national registers. Within both study arms, no significant difference was observed between QALYs and cost measures. The observed cost increase with respect to informal care was not outweighed by the savings in the formal care sector [22].

Gitlin et al. [23] examined the cost-effectiveness of a structured intervention administered by an occupational therapist composed of six in-home sessions and two telephone contacts over a period of 4 months (see Table 5). The intervention was structured into 3 parts: firstly the capabilities of the PwD were assessed. Secondly, an identification of activities that are tailored to the prevailing capabilities of the PwD was conducted and caregivers were instructed on support strategies. Eventually, when the activities were mastered, the occupational therapist was giving advice on how to employ the practiced techniques to other care challenges. The intervention reduced the time the caregiver was occupied by activities provided in relation to the PwD and was found to be cost-effective compared to treatment as usual.

Six publications were found that focused on five interventions mainly delivered to informal caregivers of PwDs (see Table 6) [18, 19, 29‐32].

A Dutch CEA and CUA conducted by Joling et al. [29] evaluated the effectiveness of a family meetings intervention on caregiver’s mental health compared to CAU from the societal perspective. Data was gathered alongside a RCT of 192 primary caregivers of community-dwelling PwD. The intervention consisted of two individual meetings between the caregiver and a trained counsellor and four structured family meetings with additional relatives and friends joining in. Apart from the scheduled sessions, the counsellor was available for support via telephone. The objective of the family meetings was to provide psychoeducation, problem solving techniques and to mobilize the existing family networks. However, after 12 months, significant effects on caregiver’s depression and anxiety could not be observed. The same applies for caregiver’s and patient’s quality of life. Further, over the 12 months, no significant cost difference between the intervention and control group was measured. Total cost per patient-caregiver dyad was estimated to be EUR 77,832 in the family meetings group compared to EUR 75,201 in the CAU group (mean adjusted difference EUR 4,149; 95% CI: -13,371 to 21,956; ICER 157,534). Hence, the researchers drew the conclusion that compared to CAU the provision of family meetings cannot be considered a cost-effective strategy.

A Swedish CUA by Dahlrup et al. [30] evaluated the cost-effectiveness of a psychosocial intervention for family caregivers of PwDs including five weekly counselling sessions administered by a registered nurse and a counselor. Education and information on dementia as well as available services in the community were followed by a group discussion. Caregivers who were unable to join group sessions received individual meetings and were invited to continue the support groups twice a month over a period of three months. 12 months after the fifth educational session, a follow-up was offered for each group. Over the time span of the study, caregivers in the intervention group were given the opportunity to contact a physician, the administering nurse or the counselor. With regard to the endpoints survival and time to institutionalization of the PwD, the intervention group did not differ significantly from the control group with CAU. A subgroup analysis based on the relation between caregiver and PwD was conducted, which demonstrated that if the caregiver was a spouse or cohabitant, PwDs transition into the nursing home occurred earlier compared to the control group (p < 0.01). In case the caregiver was a child or grandchild of a PwD, patients in the intervention group stayed longer in the community compared to controls (p = 0.06). The analysis of caregiver’s Health Related Quality of Life (HRQoL) was distinguished into caregivers whose care recipient was still living in the community and PwDs that had moved to a nursing home. For the former subgroup, caregiver’s health-related quality of life measured by EQ-5D was significantly higher in the intervention group compared to the controls. There was no significant in between-group difference with regard to caregivers whose care recipient moved to a nursing home. Depending on the caregiver’s relation to the care recipient, HRQoL differed. Resource use for home help services, nursing home care and the study intervention were collected. The cost analysis accounted for the differing length of observation. Over the 5-year follow-up, the median total cost weighted for study length did not differ between the two groups under consideration. For the intervention group the median total cost per month amounted to EUR 1,926 (interquartile range 1,043 to 2,588) in comparison to EUR 1,860 (interquartile range 864 to 2,577) in the control group (p = 0.47). Hence, it can be concluded that the intervention yielded significantly higher HRQoL in children and grandchildren caring for a PwD without significantly increasing the evaluated cost (i.e. costs for home help services, nursing home placement and the intervention cost).

An American cost analysis performed by van Houtven et al. [32] evaluated the effect of skill training aiming to reduce depressive symptoms of family caregivers of persons with AD or Parkinson’s disease on the caregiver’s out-of-pocket (OOP) costs. The skill training lasted over 24 weeks and included in-home or telephone-based sessions administered by a trained nurse. The control group was composed of the wait-list participants, who received supportive consultations via phone. Van Houtven and colleagues [32] reported clinically and statistically significant reductions in depressive symptoms and positive effects on caregiving mastery for the participants in the intervention group. The cost analysis solely included OOP costs faced by the caregiver for services provided to the care recipient or the caregiver himself. The analysis indicates that the intervention increased the likelihood of caregiver’s OOP expenditure by 26% points, however no intervention effect was observed with regard to the overall level of expenditures. It was acknowledged by the authors that OOP cost form only a part of the total economic cost which caregivers may face [32].

Wray et al. [31] examined the effect of the provision of a telehealth education program to spousals of veterans with dementia in the United States of America. The telephone support group included educational aspects on the syndrome as well as training on emotion-focused and problem-focused coping strategies and was administered over a period of ten weeks. Health care utilization and cost data were retrieved from the veterans’ databases. The cost analyses showed that in the short-term, 6 months after the intervention start, the total health care costs were significantly lower in the intervention arm in comparison to the CAU control (p = 0.039). The same applies when separately considering nursing home cost (p = 0.009). Mean overall cost savings achieved in the intervention group amounted to $2,768 per PwD. Of these, mean nursing home cost savings per PwD were $1,059. However, over the 12-month follow-up, the decrease in total care cost was not maintained.

Livingston and colleagues [19] evaluated the short and long-term cost-effectiveness of a manual-based individual coping strategy intervention (START) targeted at family caregivers of PwD in the UK. The manual was based on the Coping with Caregiving intervention developed in the US. The START intervention consisted of eight psychological therapy sessions, administered by psychological graduates. The sessions covered psychoeducation about dementia, caregiver stress and behavior strategies [38]. The short-term analysis over a period of 8 months with QALYs as outcome measure yielded that caregivers receiving the intervention showed higher, however non-significant, health and social care costs amounting to £252 (95% CI: £28 to £565) compared to CAU and an incremental QALY gain of 0.042 (95% CI: 0.015 to 0.071). With the total score of the Hospital Anxiety and Depression Scale (HADS-T) as outcome the incremental health and social care costs were estimated to be £247 (95% CI: £0 to £569) higher in the START group. The ICUR was £6,000 per additional QALY and £118 per unit change on HADS-T. The likelihood that the START intervention was cost-effective at a willingness-to-pay threshold of £20,000 was 93%. In the long-term (after 24 month) for the QALY analysis, the cost per additional QALY was £11,200 and the CEAC indicated that the likelihood that the intervention was cost-effective was 75% presuming a willingness-to-pay threshold of £30,000. The authors concluded that the START intervention was cost-effective over 8 and 24 months.

A second publication of Livingston et al. [18] additionally assessed PwD’s outcomes and costs. The analyses showed that when combining carer and PwD’s costs, the START intervention also dominates CAU considering caregiver’s outcomes. However, with regard to PwDs quality of life measured by means of the QoL-AD, no significant between-group difference was found.

Considering the methodological quality of the included studies, it can be acknowledged that the majority of articles gave a detailed description of the considered alternatives [see Additional file 2]. In most studies a comparison was made between a non-pharmacological intervention and CAU, whereas Davis et al. used a popular and widely available exercise program in order to reflect the actual practice in the respective community [33]. Two publications did not present detailed effectiveness results in the publication and the referenced articles could not be found [31, 32].

Regarding the methods of economic evaluations, the researchers of the identified trials most frequently applied CEA. As cost effectiveness measures, for instance, the incremental cost per one-point difference in NPI score [28] or per QoL-AD score [18, 21] were used. However, no cost-effectiveness thresholds exist for outcomes such as the change in the NPI or the MMSE score [45].

Moreover, the assessment of HRQoL in PwDs may be prone to recall bias and missing values are likely to occur within a cognitively impaired population [46]. Regarding proxy measures, a Dutch study conducted by Arons et al. indicates that patient-by-proxy HRQoL values must be interpreted cautiously, as caregivers are found to reflect parts of their own HRQoL onto the care recipient [47].

The CUAs that were included in this systematic review derived QALY of the PwD from dementia-specific instruments such as the DEMQOL and DEMQOL Proxy. Besides, generic proxy-rated caregiver EQ-5D values were employed to assess PwD’s HRQoL. Concerning the EQ-5D, a study of Aguirre and colleagues [48] suggests that the EQ-5D may not capture all relevant aspects associated with dementia and PwD’s experiences. However, Aguirre et al. [48] showed that compared to the dementia-specific measures DEMQOL and the Qol-AD, the EQ-5D demonstrated adequate psychometric properties and good reliability within this population. In addition, Orgeta et al. [49] indicated that the EQ-5D enables PwDs in mild and moderate stages to rate their own HRQoL. However, the study found significant difference between caregiver-rated and self-rated HRQoL. The ratings were influenced by the type of the caregiving relationship. Children of PwDs rated the HRQoL lower in comparison to spousal caregivers. Therefore, the authors recommend to use both self and proxy ratings in economic evaluations of interventions for PwDs [49].

In contrast, Algar and colleagues [50] propose observational measures for the effectiveness assessment of non-pharmacological interventions for PwDs. Especially, in more severe levels of dementia observational methods may provide additional valuable data and might be an alternative way to capture PwD’s experiences [50]. The use of observational tools in health economic analyses might therefore be a valuable field of research.

There are as well challenges arising with regard to the identification and valuation of costs. A systematic review on cost-of-illness studies showed that the main cost drivers in the dementia care context are informal care costs [51]. Moreover, Wimo et al. [52] point to the complex interaction between those who may benefit from the consequences of the interventions and those who finance the care. The societal perspective includes all relevant cost irrespective where they occur and where they are financed. Therefore, Wimo and colleagues [52] recommend that taking on a societal perspective is often preferable.

Another systematic review by Krol et al. [53] assessed the effect of the inclusion and exclusion of informal care cost and effects on cost-effectiveness outcomes. The authors concluded that the inclusion of informal care can have a considerable impact on cost-effectiveness outcomes [53]. Moreover, Shearer et al. [54] recommend that the methods employed to measure and value informal care should be explicitly stated. In addition, sensitivity analyses should be employed to show the variability of the results using alternative methods [54].

Even though a comprehensive literature search based on broad search terms was conducted, some papers meeting the search criteria might not have been identified. Moreover, this systematic review may be subject to a language bias, as solely publications in English and German were included.

A narrative synthesis was conducted due to the heterogeneity of the identified studies with regard to the employed health outcomes, perspectives of the analyses and time horizons. Furthermore, the study populations under examination comprised different types and severity levels of dementia. Moreover, the generalizability of the findings is limited since the identified studies were conducted in North American and European countries, with different underlying health and social care systems.

There is evidence on the effectiveness of multicomponent psychosocial interventions on the maintenance of caregivers’ psychological health [55] and delayed institutionalization of PwDs [12]. Furthermore, a recent study by Straubmeier et al. [56] shows a highly promising effect of a structured multicomponent intervention targeted at PwMCI and persons with mild to moderate dementia on their cognitive abilities and activities of daily living [56]. Future research should therefore examine the cost-effectiveness of multicomponent interventions and consider subgroups of PwDs at different disease stages. Moreover, the homogeneity of the respective caregivers should be taken into account.

Selected non-pharmacological interventions are recommended by most guidelines. However, there is still a lack of information on their dissemination as well as on facilitators and barriers of the translation of evidence on non-pharmacological interventions into practice.